Heat resistant elastomer compositions

ABSTRACT

HEAT RESISTANT ELASTOMER COMPOSITIONS ARE OBTAINED BY ADDING TO A CROSS-LINKABLE ELASTOMER COMPOSITION CONTAINING AT LEAST 5% BY WEIGHT OF AN ELASTOMER CONTAINING AN ACTIVE HALOGEN IN THE MOLECULE, PHENOTHIAZINE OR THE DERIVATIVES THEREOF.

United States Patent 3,716,602 HEAT RESISTANT ELASTGMER COMPOSITIONS Ichiro Iwami, Tsutomu Matsunaga, Sakae Inouye, Makoto Fujimori, Noriyuki Hayashi, Norio Wada, Ken Yoneyama, and Hideaki Inaba, Tokyo, Japan, assignors to Bridgestone Tire Company Limited, Tokyo, Japan No Drawing. Filed Dec. 12, 1969, Ser. No. 884,748 Claims priority, application Japan, Dec. 17, 1968,

43/ 92,046 Int. Cl. C080 11/60; C08d 5/04; C08f /40 US. Cl. 260889 4 Claims ABSTRACT OF THE DISCLOSURE Heat resistant elastomer compositions are obtained by adding to a cross-linkable elastomer composition containing at least 5% by weight of an elastomer containing an active halogen in the molecule, phenothiazine or the derivatives thereof.

The present invention relates to elastomer compositions having an improved thermal aging resistance and more particularly elastomer compositions having an excellent heat resistance, in which a particular effect for preventing aging is developed by synergistic function of phenothiazine and the derivatives thereof (referred to as phenothiazines hereinafter) and a halogen-containing elastomer.

Phenothiazines have been interested as a stabilizer for lubricants to be used for a high temperature and in some cases have been tested as an antioxidant for rubber but they are not particularly excellent as compared with conventional stabilizers and antioxidants and have defects in the inherent properties, therefore they heretofore have not been used practically.

The inventors have found that the phenothiazines show a synergistic elfect together with active halogen-containing elastomer and develop a particular effect for preventing aging and have found novel elastomer compositions having a heat resistance.

In general, there are two tendencies in variation of physical properties of elastomers due to the thermal aging. That is, one tendency is hardening in which modulus and hardness increase and the other tendency is softening depending upon ditferences of molecular structure of elastomer, kind of cross-linking agent-and aging condition. This is attributed to frequency of main chain breakage, rearrangement of cross-linkage structure and variation of cross-linkage density.

The effect for preventing aging through synergistic function of phenothiazine and halogen-containing elastomer against the variation of physical properties due to the thermal aging of elastomer involves prevention of main chain breakage owing to oxidation of elastomer and suppression of variation of cross-linked portions, whereby the hardening or softening of the vulcanized elastomer composition can be prevented. As the result, the breaking property based on crack occurrence and crack growth owing to hardening of vulcanized elastomer composition, which is used for heat resistance can. be improved and reversely the softening abrasion and blow out owing ice to softening can be prevented. Furthermore, the elastomer composition of the present invention is remarkable in the effect for preventing aging in environment at an extremely high temperature of about 120200 C., at which general antioxidants for rubber lose their function.

The heat resistant elastomer compositions of the present invention comprise adding to cross-linkable elastomer composition containing 5 to by weight based on the raw rubber components, of elastomer containing active halogen in the molecule, not more than 8% by weight based on the amount of all the rubber of phenothiazine or phenothiazine derivatives.

The phenothiazine derivative to be used in the invention is shown by the following general formula wherein R and R represent same or dififerent alkyl, alkoxy or thioalkyl groups, and one of R and R may be hydrogen atom. The phenothiazine derivative includes 3-methylphenothiazine, 2 ethylphenothiazine, 3 ethylphenothiazine, 2-t-butylphen0thiazine, 3,7-dimethylphenothiazine, 3,7-dibutylphenothiazine, 3,7-dioctylphenothiazine, l-methoxyphenothiazine, Z-methoxyphenothiazine, 3-methoxyphenothiazine, 4-methoxyphenothiazine, 2-sec butoxyphenothiazine, 3-octyloxyphenothiazine, 3-dodecyloxyphenotbiazine, 3-hexa-decyloxyphenothiazine, 3,7-dimcthoxyphenothiazine, 2,8-dimethoxyphenothiazine, 3,7- bis(octyloxy)phenothiazine, 2 methylthiophenothiazine, 3-methylthiophenothiazine, 2-isopropylthiophenothiazine, 2-sec-butylthiophenothiazine, 2-isobutylthiophenothiazine, 3-octyl-7-octyloxyphenothiazine, etc.

As the active halogen-containing elastomer, mention may be made of polychloroprene rubber, chlorosulfonated polyethylene rubber, halogenated isoprene/isobutene copolymer rubber, polyepichlorohydrin rubber, epichlorohydrin/ethylene oxide copolymer rubber, halogenated ethylene/propylene/diene terpolymer rubber, halogenated ethylene/propylene copolymer rubber, halogenated polyethylene rubber, fluorine-contained rubber, etc.

In order that the above-mentioned elastomer containing halogen in the molecule and the phenothiazine derivative develop a synergistic eifect, it is not always necessary that all the raw material elastomer component in an elastomer composition is halogen-containing elastomer. A blend of a halogen-containing elastomer with an elastomer containing no halogen may develop the synergistic elfect. In a blend of a halogen-containing elastomer with an elastomer containing no halogen, it is desirable that the halogencontaining elastomer is contained in an amount of at least 5% by weight based on the raw elastomer component in order that halogen-containing elastomer and phenothiazine develop a synergistic effect.

An amount of phenothiazine to be added in the present invention is not more the. 4% by weight based on the raw elastomer. The eifect for preventing aging increases remarkably up to 3% by weight, as the amount of phenothiazine added increases, and the effect increases by increasing the amount in more than 3% by weight, but if the amount exceeds 4% by weight, a blooming phenomenon occurs noticeably and such amount cannot be used in practice.

An amount of phenothiazine derivatives to be added in the invention is not more than 8% by weight based on the raw elastorner. The effect for preventing aging increases as in the case of phenothiazine, as the amount of phenothiazine derivative added increases. Moreover, a blooming phenomenon does not occur. However, addition of more than 8% by weight is not suitable in practice.

The synergistic effect of the phenothiazines and the halogen-containing elastomer develops independently of the kinds of compounding agents, such as filler, softener, cross-linking agent, etc. in the elastomer composition and their compounding recipe. When a dehalogenating crosslinking agent is used as a cross-linking agent, the synergistic eifect of the phenothiazines and the halogen-containing elastomer develops more remarkably. This effect for activating the synergistic effect of phenothiazines by the addition of a dehalogenating cross-linking agent is also observed in a case when the dehalogenating cross-linking agent is used together with other commonly used crosslinking agent, for example, a dehydrogenating cross-linking agent.

The cross-linkage in a halogen-containing elastomer generally proceeds due to the formation of halogen radicals or hydrogen halide resulting from dehalogenation.

As the dehalogenating cross-linking agent, which causes cross-linkage in a halogen-containing elastomer by the above mechanism, use may be made of various conventional cross-linking agents, for example, polyamines, polyamine carbamates, dimercaptans, thioureas, dioxyaromatics, derivatives of dioxy aromatics, such as di-o-tolylguanidine salt of dicathecol and oxides of polyvalent metals.

An amount of the dehalogenating cross-linking agent to he added can be selected optionally within the range that is commonly used in the dehalogenating cross-linkage in halogen-containing elastomer.

With respect to the mechanism of synergistic effect of the phenothiazines and halogen-containing elastomer, halogen presumably takes a part in the activation of the phenothiazines at their cation radical formation. Particularly, when dehydrogenating cross-linking agent is used, halogen ion or radical acts more strongly, and therefore the activating effect of the halogen-containing cross-linking agent against the phenothiazines develops more remarkably, but the mechanism is not clear at present.

The following examples are given in illustration of this invention and are not intended as limitations thereof. Examples 1, 2, 3, 4 and 7 show the effect of phenothiazines added to a rubber composition, in which all the raw elastomer component is halogen-containing elastomer. Examples 5 and 6 show the effect of phenothiazines added to an elastomer composition, in which the raw elastomer component is a mixture of a copolymer containing active halogen and that containing no active halogen. The numerical value in the compounding recipe means part by weight.

EXAMPLE 1 This example shows the effect of phenothiazine added to an elastomer composition wherein a chlorinated isoprene/ isobutene copolymer (hereinafter abridged as chlorinated HR) was used as a halogen-containing elastomer and a thiuram or sulfur, which is commonly used as a dehydrogenating cross-linking agent, was used.

(1) Compounding recipe Con- Chlorinated HR 1 Carbon black (HAF grade) 1 HT1066, made by Esso Co.

(2) Conditions for preparing test samples.-

Vulcanization condition: C. X 60 minutes. Aging condition: JIS No. 1 dumbell specimen is left to stand for 1 Abbreviation of Japanese Industrial Standard. Hereinafter this abbreviation will be used.

As seen from the result when phenothiazine is not added, if the resulting composition is aged in air at C., the effective density of networks lowers and the elastomer composition softens. On the other hand, when phenothiazine is added, the networks are stabilized and the softening is prevented. Moreover, the elastomer composition after aging is somewhat higher than that before aging in 300% modulus. The tensile strength is maintained favourably.

EXAMPLE 2 This example shows the effect of phenothiazine added to an elastomer composition, wherein a dehydrogenating cross-linking agent was used for a halogen-containing elastomer.

( 1) Compounding recipe Ctori- Cm;- Con; r0 r0 trol Composition. 2-1 2-1 2-2 2-2 2-3 2-3,

Chlorinated HR 1 100 100 Polyehloroprene rubber 7 100 100 Epiehlorohydrin rubber 3 100 100 Carbon black (FEF grade)... 50 50 50 50 50 Steane aei 1 1 1 1 Spindle oil 8 8 8 8 Zinc white 5 5 5 5 Magnesium oxide 2. 5 2. 5 2. 5 2. 5 Hexamethylenediamine carbamate 2. 5 2. 5 2-mercaptoimidazolineethylenethiourea 0. 7 0. 7 1. 0 1. 0 Pentaery 5. 0 5. 0 Phenothiazine 2.0 3. 0 3. 0 Tetrathiuramthiourea 0. 3 0. 3

1 HT1066, made by Esso Co. 3 Neoprene W, made by Du Pont Co. I Made by Hercules Co.

(2) Conditions for preparing test samples (l) Compounding recipe Control Control 2-1 2-1' 22 2-2' 2-3 2-3' Composition 3-1 3-1 3-1 3-2 3-2 3-2" vulcanization condition:

140 O.X(m.ins 60 60 60 5 Polychloroprene rubber 100 100 100 100 100 100 145 C. (mins.) 45 45 Carbon black (GPF grade). 50 50 50 50 50 50 Aging condition .118 No. 1 dumbell specimen is left to ,TCP 1 .1.. 10 10 10 10 10 stand for 48 hours in air at 150 C. Magnesium oxide-.. 4 4 4 4 4 4 Z-mercaptoimidazoli e 0.35 0.35 0.35 Diphenylguanidine- 1 1 Sulfur r 1 1 1 10 Zinc white--- 5 5 5 5 5 5 Dioctylpheno iazine 1 l (3) Result Phenothiazine 1 1 1 Neoprene W made by Du Pont 00. Con- Con- Coni 2 1 g 2 2 2 g; 2 3 g g} Tricresyl phosphate. Com osit on 1 p s (2) Conditions for preparing test samples Physical properties:

Before aging: vulcanization conditions: 155 C. 4O mmutes.

Hardness degrees, Aging condition: J IS No. 3 dumbell specimen is left to stand for 24 HS 56 57 70 73 80 82 hours in air at 150 C. Elongation at break (percent)... 450 470 280 235 310 290 (3) Result Tensile strength k .lcmfl) 175 169 292 266 172 155 c n control 300% modulus (kg/cm!) 117 112 Compositionm. 3-1" 3-2 3-2 3-2" After aging:

Hardness degrees, Physical properties: JIS 63 70 80 90 84 91 efore aging: Elongation at Hardness degrees,

break (percent).-. 420 330 230 60 2 0 90 J1 58 56 60 60 59 52 Tensile strength Elongation at break (kg/0111. 149 128 265 109 189 170 (percent) 370 410 340 355 365 355 300% modulus Tensile strength kg /cm. 119 gJcrn. 200 210 205 200 135 210 Out growth 300% modulus at 10 1, 230 (kg-[0111 180 166 195 181 175 195 After aging: Hardness degrees,

JIS 68 67 72 74 74 78 Elzmgatiotr; at break 6 ercen 1 o 195 55 100 115 6 As seen from the above table, when phenothiazine 1S 535 Strength 0 added, the decrease of elongation of the elastomer com- 8 5 5132 32 36 75 position by aging is considerably suppressed, and fur- (kg/cm?) ther the changes of hardness and modulus of elasticity by aging is very small. As the result, the out growth As seen from the above table, when phenothiazine or resistance of the elastomer composition is remarkably its derivative is not added, if the resulting elastomer comi d, position is aged in air at 150 C., the elastomer com- That is, when the elastomer composition cross-linked position remarkably hardens. On the other hand when by a diamine is aged, it forms secondary networks more phenothiazine or its derivative is added, the hardening easily than the elastomer composition cross-linked by is prevented, and moreover the tensile strength is main a thiuram or sulfur in Example 1, and apt to harden. talned favorably. However, when elastomer compositions added with The molecular weight of dioctylphenothiazine is about phenothiazine are aged, the secondary cross-linking due 2 tunes that of phenothiazine, and when dioctylphenoto the aging can be prevented. Thus, phenothiazine can thiazine or phenothiazine is added in the same amount, stabilize the network structure in both of the elastomer substantially the same effect can be attained. This fact compositions added with diamine, or thiuram or sulfur. shows that dioctylphenothiazine has an eiiect for pre- EXAMPLE 3 venting aging remarkably higher than phenothiazine. ThlS example shows the eifect of phenothiazine or XAMPLE 4 phenothiazine derivative added to elastomer composi- This example shows the effect of phenothiazine or its tions, wherein polychloroprene rubber was used as a derivative added to various halogen-containing elastomer halogen-containing elastomer. compositions.

(1) Compounding recipe Control Control Control Composition 4-1 4-1 4-1" 4-2 4-2 4-2" 4-3 4-3 4-3" Polychloroprene rubber l 100 Chlorosulfonated polyethylene rubber 100 100 100 Chlorinated HR3 100 100 100 Carbon black (GPF grade) 50 TOP 10 2-mercaptoimldazo1i Zinc white 5 5 5 5 5 6 Dloctylphenothiazine 2-1 2. 1 2. 1 Phenothlazlne. 1 1 1 1 Neoprene GRT, made by Du Pont Co. Hypalon 29, made by Du Pont Co. HT1066, made by Esso Co.

(3) Result (2) Conditions for preparing test samples Control Vulcanization condition: 155 C.X4O minutes Compgsiflon H Agmg condmon: 5 Physical properties:

Polychloroprene rubber and chlonosulfonated poly- Before agmgt Hardness (degrees) (HS) 60 59 60 64 62 ethylene rubber composition are left to stand for glonglafign P g gg 23 $22 3 615 o ensi e s ren g. cm. 1 1 180 v 24 hours In 1 300% modulus (kg/cm!) -4 s4 s9 60 70 70 Chlorinated IIR composition is left to stand for 24 hours After s e o 10 Hardne 67 73 75 74 In at 150 495 340 310 320 180 175 200 197 300% modulus (kg/cm!) 98 170 190 187 (3) Results Control Control Control Composition 41 4P-1' 4-1" 4-2 4-2 4-2" 4-3 4-3 4-3" Physical properties:

Betorea ing:

Har ness (JIS) 61 62 63 66 66 66 44 45 43 Elongation at break (percent) 365 370 300 300 295 285 480 430 386 Tensile strength (kg./

031. u nnd nlnm 190 200 190 220 220 220 125 120 115 300 me us g.

mi!) 182 186 86 94 97 After aging:

Hardness (IIS) 65 65 66 69 68 69 47 49 4s Elongation at break (percent) 265 280 235 285 260 245 520 450 440 Tensile strength (kg.l

c1112 l 175 150 170 210 210 230 82 86 86 300 mo ulus 031. g 54 e5 69 Cut growth index at As seen from the above table, the outgrowth resistance of all the polychloroprene rubber, chlorosulfonated polyethylene rubber and chlorinated IIR compositions is improved by the addition of phenothiazine or its derivative.

EXAMPLE 5 This example shows the eifect of phenothiazine added to ethylene/propylene terpolymer rubber (hereinafter abridged as EPT rubber) composition.

In this example, EPT rubber was blended with chlorinated HR, because EPT rubber does not dontain active halogen. Further, the effect of a dehalogenating agent to the blended chlorinated HR is shown.

For comparison, samples, wherein chlorinated HR is not blended, are shown.

{1) Compounding recipe (2) Conditions for preparing test samples.-

Vulcanization condition:

vulcanization Aging condition: 150 C. 48 hours, left to stand in air 140 C. 60 minutes, press As seen from the above table, EPT rubber composition shows a typical hardening-type aging, wherein the hardness and modulus considerably increased, and the elongation lowers by thermal aging. Even if an EPT rubber composition is blended with a small amount of chlorinated IIR, these properties remain unchanged. However, when phenothiazine is added to EPT rubber composition blended with chlorinated II R, the hardening by heat of the rubber composition is considerably suppressed. In the sample wherein diamine carbamate having dichlorinating ability of the blended chlorinated HR is added and the resulting mixture is vulcanized, the elfect of phenothiazine is more improved.

As seen from the comparison, in the EPT rubber composition, Which is not blended with chlorinated HR, addition of phenothiazine is not efiective.

EXAMPLE 6 This example shows the effect of various phenothiazine derivatives added to EPT rubber composition. The EPT rubber was blended with chlorinated DR, because the EPT rubber does not contain active halogen.

(1) Compounding recipe 1 EPTSOI, made by Uniroyal Co. I HT1066, made by Esso 00. Sumilite PEP-19900, made by Sumitomo Bakelite Co.

2) Conditions fior preparing test samples Vulcanization condition: C. 60 minutes, press vulcanization Aging condition: 0X24 hours, left to stand in hot air (3) Result Composition. 6-1 6-2 6-3 6-4 6-5 6-6 6-7 6-8 6-9 Control Phenothlazines:

3-t-butylphenothiazine-.- 1 5 3. 4. 3,7-di-t-butylphenothiazin l. 5 3. 0 3,7,(11-oety1pheno Phenothimina Physical properties:

Beiore aging:

Hardness (degrees) (HS) 60 60 58 59 58 59 58 58 58 60 60 60 Elongation at break (percent) 535 540 585 555 565 555 540 550 560 465 495 510 Tensile strength (k .lcmfl) 100 95 105 95 105 110 95 100 105 95 100 99 300% modulus (kgfimfl) 61 56 56 55 61 59 55 59 55 66 68 56 Blooming No No No No No No No No Yes No Aiter aging:

Hardness (degree) (JIS) 67 66 64 67 65 64 66 62 60 68 69 68 Elongation at break (percent) 360 475 480 400 465 510 385 420 470 380 360 320 Tensile strength (k .lcmfl) 105 90 75 105 90 75 105 95 80 105 100 110 300% modulus (kg. gm?) 64 53 92 68 53 91 79 59 100 95 Cut growth index at 100 C- 360 515 420 360 515 375 290 455 420 145 285 100 I Aiew. 1 Remarkable.

As seen from the above table, elastomer composition, wherein EPT rubber is blended with a small amount of chlorinated 11R, hardens by thermal aging, and causes lowering of out growth resistance.

It can be seen that as the amount of each phenothiazine derivative added is increased, the hardening of the elastomer composition by heat is more suppressed. However, when phenothiazine is added in an amount of 1.0% by weight, a blooming phenomenon occurs, and in addition of 1.5% by weight such a phenomenon becomes remarkable, so that the etfect of phenothiazine cannot be maintained for a long period of time.

On the other hand, even when alkyl-substituted phenothiazine is added in an amount up to 4.5% by weight, a blooming phenomenon does not occur, and further the hardening of elastomer composition is considerably suppressed.

EXAMPLE 7 This example shows the effect of phenothiazine derivative added to halogen-containing elastomer.

(1) Compounding recipe Composition. 7-1 7-2 7-3 Dioctylphenothiazine 3 Tetrachloropheno 3 1 HT1066, made by Esso Co.

(2) Conditions for preparing test samples Vulcanization condition: 155 C x 40 minutes Aging condition: left to stand for 24 hours in air at 150 As seen from the above table, the effect of phenothiazine derivative added to halogen containing elastomer is remarkable.

For comparison, the eifect of antioxidants other than phenothiazines, and the effect of phenothiazines added to elastomer composition, wherein the raw elastomer contains no active halogen, will be described in the following Comparative Examples 1 and 2.

Comparative Example 1 This example shows the effect of phenothiazine and that of commonly used typical antioxidants other than phenothiazines added to the chlorinated butyl rubber composition used in Example 2. As a phenol series antioxidant, 2,2-methylene-bis(4 methyl-t butyl phenol) (hereinafter abridged as antioxidant A) is used. As an amine series antioxidant, 2,2,4-trimethyl 1,2 dihydroquinoline polymer (hereinafter abridged as antioxidant B) and phenyl-fi-naphthylamine (hereinafter abridged as antioxidant C) were used. The amount of antioxidant to be added was 2% by weight based on raw elastomer in the elastomer composition.

Vulcanization condition and aging condition were same with Example 1.

The obtained result is shown in the following table.

As seen from the table, the effect of these antioxidants is extremely inferior to that of phenothiazine, and particularly the effect of amine series antioxidant is not observed at all.

Control Composition 2-4 2-1 1 8-1 1 8-2 1 8-3 3 Physical properties: Before aging:

Hardness (degrees) (JIS) 56 57 55 59 60 Elongation at break (percent) 460 470 460 450 470 Tensile strength (kg./om. 175 169 172 169 170 300% modulus (kgJcmfl) 117 112 120 117 115 After aging:

Hardness (degrees) (J IS) 63 70 69 76 72 Elongation at break (percent)-.. 420 330 330 230 230 Tensile strength (kgJemfl) 149 128 130 129 111 300% modulus (kg/cmfi)... 11 142 Cut growth index at 100 C 100 200 100 125 1 Added with antioxidant A. 1 Added with antioxidant B. 3 Added with antioxidant 0.

Comparative Example 2 (1) Compounding recipe Composition Control, 9-1

SB R #1500- Carbon black (HAF grade).. Stearie acid Spindle oil. Zinc white Control, 9-2

ul ur Phenothiazine.

(2) Conditions for preparing test samples 1 1 vulcanization condition: 140 C. 45 minutes Aging condition: JIS No. 1 dumbell specimen is left to stand for 48 hours in air at 150 C.

(3 Result Composition Control, 9-1 Control, 9-2

Before aging:

Hardness (degrees) (I IS) 54 56 Elongation at break (percent) 605 585 Tensile strength (kgJemJ) 261 258 300% modulus (kg./en1. 94 104 After aging:

Hardness (degrees) (I IS) 67 68 Elongation at break (percent) 315 280 Tensile strength (kg/0111. )".v 215 194 300% modulus (kg/c1113.".-.

As seen from the above table, the effect of phenothiazine added to halogen-containing elastomer is not observed in elastomer containing no halogen.

What is claimed is:

1. A vulcanizable composition comprising (a) a rubber cross-linking agent selected from the group consisting of a mixture of at least one of sulfur and tetramethylthiuram disulfide and at least one of heXamethyiene-diamine carbamate and magnesium oxide,

(b) a rubber consisting of not more than 95% by weight of ethylene-propylene-diene terpolymer and 5 to 100% by weight of chlorinated isoprene-isobutene copolymer,

(c) not more than 8% by weight based upon the rub ber of phenothiazine or a phenothiazine derivative having the general formula wherein at least one of R and R is selected from the group consisting of alkyl, alkoxy, thioalkyl, halogenated alkyl, halogenated alkoxy, and halogenated thioalkyl group having 1 to 18 carbon atoms.

2. The elastomer composition of claim 1, wherein said phenothiazine derivative is alkylated phenothiazine.

3. The elastomer composition of claim 2, wherein said alkylated phenothiazine is selected from the group consisting of dioctylphenothiazine, mono-t-butylphenothiazine and di-t-butylphenothiazine.

4. A vulcanizate obtained by heat curing the vulcanizable composition of claim 1.

References Cited UNITED STATES PATENTS 1,809,798 6/1931 Cliiford 260800 1,950,442 3/1934 Williams et a1. 26092.3 1,967,863 7/1934 Collins et a1. 260--92.3 2,630,398 3/1953 Brooks et a1 26079.3 2,732,354 1/ 1956 Morrissey et a1 2605 2,815,336 12/1957 Freytag et al. 260-923 2,962,475 11/1960 Malz et al. 26045.8 2,983,707 5/1961 Baldwin et a1. 260-45.9 3,297,660 1/ 1967 Becker 260--79.5 3,364,170 1/ 1968 Savides 260--45.8 3,028,346 4/1962 Lemiszka et a1 2605 3,163,626 12/1964 Mindkler, Jr., et a1. 260-85.3 3,343,582 9/1967 Himes et al. 152-330 3,454,462 7/ 1969 Hawley 161-243 3,534,123 10/1970 Bostock et al 260-888 3,580,867 5/1971 Spenadel 2602.5 3,630,974 12/1971 Ladowi et al. 260-5 OTHER REFERENCES Hofmann, Vulcanization and Vulcanizing Agents, 1967, pp. 13-15, section 1.1.2.11.l.

DONALD E. CZAIA, Primary Examiner R. A. WHITE, Assistant Examiner US. Cl. X.R.

2-6045.8 SN, 79.5 A, 85.3 C 

